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Novus Biologicals
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Enzo Biochem
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ImmunoTools
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List Biological Laboratories
toll-like receptor [tlr]4 ligand lipopolysacharide [lps] ![]() Toll Like Receptor [Tlr]4 Ligand Lipopolysacharide [Lps], supplied by List Biological Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/tlr4+ligand/toll+like+receptor++tlr+4+ligand+lipopolysacharide++lps+/pm25240680-44-23-34 Average 90 stars, based on 1 article reviews
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Verlag GmbH
lipid a (tlr4 ligand) ![]() Lipid A (Tlr4 Ligand), supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/tlr4+ligand/lps++tlr4+ligand++from+e++coli+0+111+b4/pm20201020-335-0-16 Average 90 stars, based on 1 article reviews
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InvivoGen
2’3’-cgamp ![]() 2’3’ Cgamp, supplied by InvivoGen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/tlr4+ligand/2%E2%80%993%E2%80%99-cGAMP/custom%40tlrl-nacga23-02%4010%2E1016%2Fj%2Ecelrep%2E2023%2E112306 Average 99 stars, based on 1 article reviews
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BioChem GmbH
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Avanti Polar
3d(6-acyl) phad ![]() 3d(6 Acyl) Phad, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/tlr4+ligand/3D(6-acyl)+PHAD/custom%40699855p%4038968676 Average 94 stars, based on 1 article reviews
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Joint Research Center
human toll-like receptor 4 (tlr4) ligands ![]() Human Toll Like Receptor 4 (Tlr4) Ligands, supplied by Joint Research Center, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/tlr4+ligand/human+toll+like+receptor+4++tlr4++ligands/pm21262374-9-71-114 Average 90 stars, based on 1 article reviews
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Lipopolysaccharide-LPS from Ecoli 0111:B4, TLR4 ligand
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Image Search Results
Journal: Cell Discovery
Article Title: Structure of the full-length human Pannexin1 channel and insights into its role in pyroptosis
doi: 10.1038/s41421-021-00259-0
Figure Lengend Snippet: a Schematic representation of hPANX1 heptamer in light blue docked into the cryo-EM density map. The middle panel shows the top view of hPANX1 with glycosylation indicated. The right panel shows a magnified view of the N-linked glycans (including two N-Acetylglucosamine and eight Mannose). b Representative images of the localization of WT and N255Q hPANX1 in THP-1-derived macrophages (MPs). The images were collected using the super-resolution STED mode. OE is the abbreviation of overexpression in all the figures. Scale bar = 5 µm. c Western blot analysis of the NLRP3 and Pro-IL-1β in WT hPANX1 overexpressing and N255Q hPANX1 overexpressing MPs. MPs were treated with LPS (1 µg/ml) and ATP (3 mM) for 24 h. GAPDH was used as a loading control. d IL-1β release from mock, WT hPANX1 overexpressing and N255Q hPANX1 overexpressing MPs. MPs were primed with LPS (1 µg/ml) overnight and stimulated with nigericin (10 µM) for 0.5, 1, or 2 h. IL-1β release was measured by ELISA. Error bars represent s.e.m. for n = 3. * P < 0.05, NS not significant (one-way ANOVA followed by Dunnett’s test, OE WT set as comparison control). e Phase-contrast images of MPs stimulated by LPS and ATP. Images were acquired with an IncusyteS3 system on day 6. f Time course of live cell confluence of MPs. Image data were collected every 2 h and analyzed with an IncusyteS3 system. Error bars represent s.d. for n = 4. *** P < 0.001, **** P < 0.0001 (one-way ANOVA followed by Dunnett’s test, OE WT set as comparison control).
Article Snippet: To differentiate THP-1 cells into macrophages (MPs), 50 ng/ml phorbol 12-myristate 13-acetate (PMA, Sigma-Aldrich, P1585–1MG) was added to the growth medium and maintained for 24 or 48 h. THP-1 derived MPs were stimulated for the indicated time with 30 μM R848, pHrodo E. coli bioparticles (Life Technologies, P35361), 1 μg/ml
Techniques: Cryo-EM Sample Prep, Glycoproteomics, Derivative Assay, Over Expression, Western Blot, Control, Enzyme-linked Immunosorbent Assay, Comparison
Journal: Cell Discovery
Article Title: Structure of the full-length human Pannexin1 channel and insights into its role in pyroptosis
doi: 10.1038/s41421-021-00259-0
Figure Lengend Snippet: a Representative images of the localization of WT and mutant hPANX1 (D379A and S424A) in MPs. The images were collected using the super-resolution STED mode. Scale bar = 5 µm. b Western blot analysis of the NLRP3, Pro-IL-1β in WT and mutant (D379A and S424A) hPANX1 overexpressing MPs. MPs were treated with LPS (1 µg/ml) and ATP (3 mM) for 24 h. GAPDH was used as a loading control. c IL-1β release from mock, WT overexpressing and mutant (D379A and S424A) overexpressing MPs. MPs were primed with LPS (1 µg/ml) overnight and stimulated with nigericin (10 µM) for 0.5, 1, or 2 h. IL-1β release was measured by ELISA. Error bars represent s.e.m. for n = 3. * P < 0.05, ** P < 0.01, NS not significant (one-way ANOVA followed by Dunnett’s test, OE WT set as comparison control). d Phase-contrast images of MPs stimulated by LPS and ATP. Images were acquired with an IncusyteS3 system on day 6. e Time course of live cell confluence of MPs. Image data were collected every 2 h and analyzed with an IncusyteS3 system. Error bars represent s.d. for n = 4. *** P < 0.001, **** P < 0.0001 (one-way ANOVA followed by Dunnett’s test, OE WT set as comparison control).
Article Snippet: To differentiate THP-1 cells into macrophages (MPs), 50 ng/ml phorbol 12-myristate 13-acetate (PMA, Sigma-Aldrich, P1585–1MG) was added to the growth medium and maintained for 24 or 48 h. THP-1 derived MPs were stimulated for the indicated time with 30 μM R848, pHrodo E. coli bioparticles (Life Technologies, P35361), 1 μg/ml
Techniques: Mutagenesis, Western Blot, Control, Enzyme-linked Immunosorbent Assay, Comparison